Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED NA

Assessment of Feeding Tolerance in Infants Fed Cow Milk Formula

NCT00666120 · View on ClinicalTrials.gov ↗

Study Summary

To compare the number of infants who discontinue from study formula due to formula intolerance as documented by the investigator. Hypothesize there will be no difference between formula groups.

Interventions

  • OTHER Enfamil LIPIL with iron
  • OTHER Good Start Supreme with DHA and ARA

Study Locations (18)

Arkansas

  • Harvey Pediatrics — Jonesboro
  • Mercy Rogers Pediatric Clinic — Rogers

Florida

  • Tampa Bay Medical Research — Clearwater
  • Children's Medical Association — Tamarac

Kentucky

  • Pediatrics Clinical Trials Unit — Louisville
  • Pedia Research — Owensboro

Nebraska

  • The Center for Human Nutrition — Omaha
  • Boystown — Omaha

California

  • Lovelace Scientific Resources — Santa Ana

Illinois

  • Children's Health Care — DeKalb

Indiana

  • Welborn Clinic — Evansville

Iowa

  • Fomon Infant Nutrition Unit — Iowa City

Trial Details

FieldValue
Enrollment Target 333 participants
Start Date 2005-06
Est. Completion 2006-04
Phase NA

Sponsor

Mead Johnson Nutrition

6 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00666120

The ClinicalTrials.gov registry entry for NCT00666120 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 333 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mead Johnson Nutrition, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Healthy Term Infants Solely Formula Fed appearing as the primary indexed condition, and to 2 interventions — of which Enfamil LIPIL with iron is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00666120 reports 18 study locations spanning 14 distinct geographic areas — top geographies include Arkansas, Florida, Kentucky. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00666120 about?

NCT00666120 is a clinical study titled "Assessment of Feeding Tolerance in Infants Fed Cow Milk Formula". To compare the number of infants who discontinue from study formula due to formula intolerance as documented by the investigator. Hypothesize there will be no difference between formula groups.

What is the current status of trial NCT00666120?

This trial is currently completed. It is a NA study. The enrollment target is 333 participants. The study started on 2005-06. Estimated completion is 2006-04.

What conditions does trial NCT00666120 study?

This clinical trial studies the following conditions: Healthy Term Infants Solely Formula Fed. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00666120?

The interventions under investigation include: Enfamil LIPIL with iron (OTHER), Good Start Supreme with DHA and ARA (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00666120?

This trial is sponsored by Mead Johnson Nutrition, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00666120 being conducted?

This trial has 18 study locations across Arkansas, California, Florida, Illinois, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial